EP2489705A1 - Production method for polymer paint with non-flammable property - Google Patents
Production method for polymer paint with non-flammable property Download PDFInfo
- Publication number
- EP2489705A1 EP2489705A1 EP12156116A EP12156116A EP2489705A1 EP 2489705 A1 EP2489705 A1 EP 2489705A1 EP 12156116 A EP12156116 A EP 12156116A EP 12156116 A EP12156116 A EP 12156116A EP 2489705 A1 EP2489705 A1 EP 2489705A1
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- EP
- European Patent Office
- Prior art keywords
- polymer
- flammable
- mixture
- paint
- huntite
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K3/2279—Oxides; Hydroxides of metals of antimony
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/18—Fireproof paints including high temperature resistant paints
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/2224—Magnesium hydroxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/016—Flame-proofing or flame-retarding additives
Definitions
- the present invention is related to the production of a paint having non-flammable property.
- polymer-based materials are preferred for reasons such as cost, strength, ease of productions.
- Polymer-based materials which are also known as plastics, are carbon compounds and can easily be processed because of their plastic properties.
- the structural strength of such materials can be adjusted at the desired levels.
- combustion resistance of these polymer-based materials is very limited. Since polymers are compounds that contain high levels of carbon, hydrogen and oxygen, they burn easily and rapidly. Combustion of polymers progress 4 times more rapidly than that of wood. During the combustion of polymers toxic and combustible gases are released together with heat. Moreover, the medium becomes more combustible when polymer chains break into smaller parts or molecules through the impact of heat. For example, during the combustion of polypropylene the propane gas, which is more combustible than polypropylene, is released. The spread of combustion depends on the severity of the combustion and the response of the polymer to this.
- the polymer has a natural combustion resistance, it is necessary that there is high level of carbonization at lower temperatures, that is has heat stability above 400 °C (high melting temperature), and that the decomposition products formed below 400 °C are non-combustible gases (CO 2 , HCl, H 2 O etc.)
- the polymer materials Upon the rise of the ambient temperature above the normal level, the polymer materials first lose their form, and in the next stage they easily burst into flames as their chemical structures are affected.
- the polymers which are rich in carbon, rapidly burn once they catch fire and cause the fire that has formed grow rapidly.
- toxic gases such as carbon monoxide and carbon dioxide are released into the atmosphere at high levels. Even if the combustion of the material is prevented, release of such toxic gases may effect the composition of the ambient air critically, causing intoxication and deaths.
- these materials must be given fire-proof or non-flammable properties. Such properties can be provided by mixing the materials with non-flammable materials. However, the content of the materials may affect the mechanical and basic chemical properties of the material. Thus, to maintain or to restore the desired mechanical and chemical properties in the material, additional processes and additional materials must be used.
- halogens are used as additives to retard combustion.
- Halogens form heavy gases during combustion, which gases prevent combustion by preventing contact of the material with oxygen.
- use of halogens is not preferred due to their damage to the environment.
- a fireproof material mixed with huntite/hydromagnesite is disclosed.
- the huntite/hydromagnesite mixture is a material which can mix with polymer materials, which is not easily flammable unlike known polymers, which on the contrary in virtue of its structure that changes when the ambient temperature increases can retard the combustion of the material into which it has been mixed. Thus, the material's time to ignition is extended and a non-flammable property is rendered.
- JP 9048899 A a rubber material manufactured by adding boric acid and antimony oxide into it is disclosed. With the mentioned mixing process, the rubber is rendered fireproof. Furthermore, the mentioned mixing gives the material antibacterial and antifungal properties.
- the production method for non-flammable polymer paint involves the steps of grinding a huntite and hydromagnesite mixture to nanometric sizes; obtaining a non-flammable material by mixing the ground huntite ve hydromagnesite mixture with the ground boric acid and/or antimony oxide mixture; and addition of the non-flammable material to the polymer paint by continuous mechanical stirring.
- the polymer paint manufactured with the developed method may be used in painting polymer materials and may extend the time to ignition of the polymer materials up to 60%. Hence, the risk of polymer materials and articles produced from these materials to catch flame is decreased.
- the object of the present invention is to provide a polymer paint production method.
- a further object of the present invention is to provide a non-flammable polymer paint production method.
- Another object of the present invention is to provide a production method for a polymer paint with good surface adhesion property.
- Another object of the present invention is to provide a production method for a polymer paint that allows the formation of a smooth surface.
- Polymer materials (plastics) used frequently in daily articles enhance the severity of the fire in a probable fire event since they easily burn and catch fire, and also pose a danger because of the toxic gases that are released during combustion. Thus, it is important to render such materials fireproof.
- boric acid is H 3 BO 3 . It is a odourless, tasteless, air-stable substance in the form of white crystals. Its molecular weight is 61.83, melting point is 169°C and boiling point is 300°C. iit has a specific weight of 1.46 g/cm 3 . Is heated up to 175°C, it loses water and becomes metaboric acid (HBO 2 ). If heated more, it is converted to tetraboric acid (H 2 B 4 O 7 ), and if heated even more it is converted to glassy boron trioxide. Boric acid is used in manufacture of heat resistant borosilicate glass and also in production of glass fibres. It may be used in protecting wooden material against air and to render fabrics flame resistant. Boric acid provides resistance to flame to cellulose materials. It removes the water molecules in cellulose before reaching the flash point an the coal formed covers the surface, preventing further burning.
- Antimony is a silver-white, fragile, solid crystalline element with weak electric and heat conductance. Due to its advantages, metallic antimony is extensively used to make alloys with lead and other metals. Antimony trioxide is used as a white paint in plastics, metal coating, ceramics and enamels, and in the paint industry, and as a non-flammable in the textile, plastics and chemical industries.
- Polymer paint manufacture is provided using the paint production method developed by the present invention. This method provides fireproof properties to the mentioned polymer paint, hence, providing fireproof or non-flammable property to the painted material.
- the method developed includes the following stages:
- the non-flammable material prepared is mixed with the polymer paint. During mixing, the paint and non-flammable material mixture is continuously agitated by mechanical means. Thus, the paint is rendered a homogenous structure.
- the ratio of the non-flammable material is %30 by volume.
- Figure 1 and figure 2 give the scanning electron microscopy image of a paint produced with the developed production method. It is observed that the polymer paint produced with the developed method has good wetting properties and a rough structure. Therefore, fire retardancy is provided to the paint, while preserving the desired properties.
- the non-flammable polymer paint produced with the abovementioned method may be applied to polymer materials by conventional means known in the art.
- This polymer paint obtained retards the burning of the material in virtue of the fireproof coating formed on the surface of the material.
- Application of the paint produced may extend the time to ignition of the polymer material up to 60%. Hence the dangers that polymer materials pose when temperature is raised are reduced.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
The production method for non-flammable polymer paint, developed by the present invention, involves the steps of grinding a huntite and hydromagnesite mixture to nanometric sizes; obtaining a non-flammable material by mixing the ground huntite ve hydromagnesite mixture with the ground boric acid and/or antimony oxide mixture; and addition of the non-flammable material to the polymer paint by continuous mechanical stirring. Application of the paint produced may extend the time to ignition of the polymer material up to 60%. Hence the dangers that polymer materials pose when temperature is raised are reduced.
Description
- The present invention is related to the production of a paint having non-flammable property.
- In many of the articles used in daily life, polymer-based materials are preferred for reasons such as cost, strength, ease of productions. Polymer-based materials, which are also known as plastics, are carbon compounds and can easily be processed because of their plastic properties. In addition, the structural strength of such materials can be adjusted at the desired levels.
- However, combustion resistance of these polymer-based materials is very limited. Since polymers are compounds that contain high levels of carbon, hydrogen and oxygen, they burn easily and rapidly. Combustion of polymers progress 4 times more rapidly than that of wood. During the combustion of polymers toxic and combustible gases are released together with heat. Moreover, the medium becomes more combustible when polymer chains break into smaller parts or molecules through the impact of heat. For example, during the combustion of polypropylene the propane gas, which is more combustible than polypropylene, is released. The spread of combustion depends on the severity of the combustion and the response of the polymer to this. In order that the polymer has a natural combustion resistance, it is necessary that there is high level of carbonization at lower temperatures, that is has heat stability above 400 °C (high melting temperature), and that the decomposition products formed below 400 °C are non-combustible gases (CO2, HCl, H2O etc.)
- Upon the rise of the ambient temperature above the normal level, the polymer materials first lose their form, and in the next stage they easily burst into flames as their chemical structures are affected. The polymers, which are rich in carbon, rapidly burn once they catch fire and cause the fire that has formed grow rapidly. Also, upon the start of the combustion of the carbonaceous structure of the polymer, toxic gases such as carbon monoxide and carbon dioxide are released into the atmosphere at high levels. Even if the combustion of the material is prevented, release of such toxic gases may effect the composition of the ambient air critically, causing intoxication and deaths.
- To prevent the mentioned dangers, these materials must be given fire-proof or non-flammable properties. Such properties can be provided by mixing the materials with non-flammable materials. However, the content of the materials may affect the mechanical and basic chemical properties of the material. Thus, to maintain or to restore the desired mechanical and chemical properties in the material, additional processes and additional materials must be used.
- In the prior art, often halogens are used as additives to retard combustion. Halogens form heavy gases during combustion, which gases prevent combustion by preventing contact of the material with oxygen. However, use of halogens is not preferred due to their damage to the environment.
- In the patent document no.
KR 20090097284 A - In the patent document no.
JP 9048899 A - The production method for non-flammable polymer paint, developed by the present invention, involves the steps of grinding a huntite and hydromagnesite mixture to nanometric sizes; obtaining a non-flammable material by mixing the ground huntite ve hydromagnesite mixture with the ground boric acid and/or antimony oxide mixture; and addition of the non-flammable material to the polymer paint by continuous mechanical stirring.
- The polymer paint manufactured with the developed method may be used in painting polymer materials and may extend the time to ignition of the polymer materials up to 60%. Hence, the risk of polymer materials and articles produced from these materials to catch flame is decreased.
- The object of the present invention is to provide a polymer paint production method.
- A further object of the present invention is to provide a non-flammable polymer paint production method.
- Another object of the present invention is to provide a production method for a polymer paint with good surface adhesion property.
- Another object of the present invention is to provide a production method for a polymer paint that allows the formation of a smooth surface.
- Application examples of the polymer paint production method developed with the present invention are illustrated in the attached figures:
-
Figure 1 ; is the scanning electron microscopy image of a polymer paint manufactured by the developed method. -
Figure 2 ; is the scanning electron microscopy image of another polymer paint manufactured by the developed method. -
Figure 3 ; is the differential thermal analysis graph of pure plastic. -
Figure 4 ; is the thermogravimetry graph of pure plastic. -
Figure 5 ; is the differential thermal analysis graph of polymer based paint known in the art. -
Figure 6 ; is the thermogravimetry graph of polymer based paint known in the art. -
Figure 7 ; is the differential thermal analysis graph of a polymer based paint produced by the production method developed by the present invention. -
Figure 8 ; is the thermogravimetry graph of a polymer based paint produced by the production method developed by the present invention. - Polymer materials (plastics) used frequently in daily articles enhance the severity of the fire in a probable fire event since they easily burn and catch fire, and also pose a danger because of the toxic gases that are released during combustion. Thus, it is important to render such materials fireproof.
- It is known from the prior art that mixing polymer materials with materials such as boric acid (H3BO3), antimony oxide (Sb2O3), huntite (Mg3Ca(CO3)4) and hydromagnesite (Mg4(CO3)3(OH)2.3H2O) provides non-flammable properties. These substances include hydroxide and the endothermic decomposition between 200 °C and 400 °C, releasing water vapour and carbon dioxide. The cooling effect of the reaction and the effect of the inert gases formed establish a ceramic-like layer on the burning surface. This layer protects the combustible surface against a future combustion and heat. However, since the mentioned mixture affects also the mechanical properties of the polymer material, it is not preferred.
- The formula for boric acid is H3BO3. It is a odourless, tasteless, air-stable substance in the form of white crystals. Its molecular weight is 61.83, melting point is 169°C and boiling point is 300°C. iit has a specific weight of 1.46 g/cm3. Is heated up to 175°C, it loses water and becomes metaboric acid (HBO2). If heated more, it is converted to tetraboric acid (H2B4O7), and if heated even more it is converted to glassy boron trioxide. Boric acid is used in manufacture of heat resistant borosilicate glass and also in production of glass fibres. It may be used in protecting wooden material against air and to render fabrics flame resistant. Boric acid provides resistance to flame to cellulose materials. It removes the water molecules in cellulose before reaching the flash point an the coal formed covers the surface, preventing further burning.
- Antimony is a silver-white, fragile, solid crystalline element with weak electric and heat conductance. Due to its advantages, metallic antimony is extensively used to make alloys with lead and other metals. Antimony trioxide is used as a white paint in plastics, metal coating, ceramics and enamels, and in the paint industry, and as a non-flammable in the textile, plastics and chemical industries.
- Polymer paint manufacture is provided using the paint production method developed by the present invention. This method provides fireproof properties to the mentioned polymer paint, hence, providing fireproof or non-flammable property to the painted material.
- The method developed includes the following stages:
- Firstly, the huntite and hydromagnesite mixture is ground to particles preferably of 100 nanometre or less. Such grinding process provides homogenous and uniform blending of the non-flammable material and the paint. Reducing the material to nanometric sizes emphasizes the non-flammable property and inhibits the undesired properties (heterogeneity, reaction inefficiency). Then, the ground huntite and hydromagnesite mixture is preferably mixed with the boric acid and/or antimony oxide mixture that has been ground in the same way. In this mixture, the huntite and hydromagnesite mixture is preferably used between 1% to 50% by volume. Thus, a non-flammable material that contains huntite, hydromagnesite, boric acid and/or antimony is obtained.
- The non-flammable material prepared is mixed with the polymer paint. During mixing, the paint and non-flammable material mixture is continuously agitated by mechanical means. Thus, the paint is rendered a homogenous structure. Preferably the ratio of the non-flammable material is %30 by volume.
-
Figure 1 and figure 2 give the scanning electron microscopy image of a paint produced with the developed production method. It is observed that the polymer paint produced with the developed method has good wetting properties and a rough structure. Therefore, fire retardancy is provided to the paint, while preserving the desired properties. - When the paint produced with the developed production method and pure polymer materials are subjected to differential thermal analysis and thermogravimetry tests, the results of which are given in
Figure 3 - 8 , it is observed that the paint produced by the developed production method catches fire much more later with respect to polymer based materials known in the art and with respect to pure polymer materials, and thus, that the paint confers non-flammable property to the material. - The non-flammable polymer paint produced with the abovementioned method may be applied to polymer materials by conventional means known in the art. This polymer paint obtained retards the burning of the material in virtue of the fireproof coating formed on the surface of the material. Application of the paint produced may extend the time to ignition of the polymer material up to 60%. Hence the dangers that polymer materials pose when temperature is raised are reduced.
Claims (5)
- A method of non-flammable polymer paint production, characterised in that it comprises the steps of;- grinding a huntite and hydromagnesite mixture to nanometric sizes;- grinding boric acid and/or antimony oxide mixture to nanometric sizes;- obtaining a non-flammable material by mixing the ground huntite ve hydromagnesite mixture with the ground boric acid and/or antimony oxide mixture;- addition of the non-flammable material to the polymer paint by continuous mechanical stirring.
- A method of non-flammable polymer paint production according to claim 1, characterised by involving the step of grinding the mixture to particles of 100 nanometre or less at the stage of grinding the huntite and hydromagnesite mixture.
- A method of non-flammable polymer paint production according to claim 1, characterised by involving the step of grinding the boric acid and/or antimony oxide mixture to particles of 100 nanometre or less at the stage of grinding the boric acid and/or antimony oxide mixture to nanometric sizes.
- A method of non-flammable polymer paint production according to claim 1, characterised by using the huntite and hydromagnesite mixture between 1% to 50% by volume at the step of mixing the huntite and hydromagnesite mixture with the ground boric acid and/or antimony oxide mixture.
- A method of non-flammable polymer paint production according to claim 1, characterised by using the non-flammable material at a ratio of %30 by volume at the step of addition of the non-flammable material to the polymer paint by continuous mechanical stirring.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TR2011/01673A TR201101673A2 (en) | 2011-02-21 | 2011-02-21 | Non-flammable polymer paint production method. |
Publications (1)
Publication Number | Publication Date |
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EP2489705A1 true EP2489705A1 (en) | 2012-08-22 |
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ID=45656143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP12156116A Withdrawn EP2489705A1 (en) | 2011-02-21 | 2012-02-20 | Production method for polymer paint with non-flammable property |
Country Status (2)
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EP (1) | EP2489705A1 (en) |
TR (1) | TR201101673A2 (en) |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0245545A (en) * | 1988-08-08 | 1990-02-15 | Furukawa Electric Co Ltd:The | Flame-retardant resin composition |
JPH05170984A (en) * | 1991-12-24 | 1993-07-09 | Sekisui Jushi Co Ltd | Low smoking flame retardant resin composition |
JPH0948899A (en) | 1995-08-02 | 1997-02-18 | Japan Synthetic Rubber Co Ltd | Flame-retardant, antimicrobial and fungiproof resin composition |
CN1146472A (en) * | 1995-09-27 | 1997-04-02 | 山东省烟台市人造革厂 | Flame retardant paint for plastic flooring |
WO1999019395A1 (en) * | 1997-10-16 | 1999-04-22 | Great Lakes Chemical Corporation | Polyvinyl chloride based plenum cable compositions |
US20070131916A1 (en) * | 2003-08-22 | 2007-06-14 | Horley Susan M | Fire retardant coating composition |
KR20090097284A (en) | 2008-03-11 | 2009-09-16 | 제이에스전선 주식회사 | Compound for intumescent flame-retardent member and flame-retardent bushing system using the same |
EP2322581A1 (en) * | 2009-11-03 | 2011-05-18 | Omya Development AG | Precipitated magnesium carbonate |
EP2355111A2 (en) * | 2010-01-27 | 2011-08-10 | King Abdulaziz City for Science and Technology | Cross-linked clean flame retardant wire and cable insulation compositions for enhancing mechanical properties and flame retardancy |
-
2011
- 2011-02-21 TR TR2011/01673A patent/TR201101673A2/en unknown
-
2012
- 2012-02-20 EP EP12156116A patent/EP2489705A1/en not_active Withdrawn
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0245545A (en) * | 1988-08-08 | 1990-02-15 | Furukawa Electric Co Ltd:The | Flame-retardant resin composition |
JPH05170984A (en) * | 1991-12-24 | 1993-07-09 | Sekisui Jushi Co Ltd | Low smoking flame retardant resin composition |
JPH0948899A (en) | 1995-08-02 | 1997-02-18 | Japan Synthetic Rubber Co Ltd | Flame-retardant, antimicrobial and fungiproof resin composition |
CN1146472A (en) * | 1995-09-27 | 1997-04-02 | 山东省烟台市人造革厂 | Flame retardant paint for plastic flooring |
WO1999019395A1 (en) * | 1997-10-16 | 1999-04-22 | Great Lakes Chemical Corporation | Polyvinyl chloride based plenum cable compositions |
US20070131916A1 (en) * | 2003-08-22 | 2007-06-14 | Horley Susan M | Fire retardant coating composition |
KR20090097284A (en) | 2008-03-11 | 2009-09-16 | 제이에스전선 주식회사 | Compound for intumescent flame-retardent member and flame-retardent bushing system using the same |
EP2322581A1 (en) * | 2009-11-03 | 2011-05-18 | Omya Development AG | Precipitated magnesium carbonate |
EP2355111A2 (en) * | 2010-01-27 | 2011-08-10 | King Abdulaziz City for Science and Technology | Cross-linked clean flame retardant wire and cable insulation compositions for enhancing mechanical properties and flame retardancy |
Non-Patent Citations (7)
Title |
---|
BIRANE TOME ET AL: "Fire resistance and mechanical properties of a huntitelhydromagnesitelantimony trioxide/decabromodiphenyl oxide filled PP-PE copolymer", POLYMER DEGRADATION AND STABILITY, vol. 53, 1 January 1996 (1996-01-01), pages 371 - 379, XP055026328 * |
DATABASE WPI Week 199013, Derwent World Patents Index; AN 1990-094616, XP002675457 * |
DATABASE WPI Week 199332, Derwent World Patents Index; AN 1993-252898, XP002675456 * |
DATABASE WPI Week 200113, Derwent World Patents Index; AN 2001-113074, XP002675474 * |
HOLLINGBERY L A ET AL: "The fire retardant behaviour of huntite and hydromagnesite - A review", POLYMER DEGRADATION AND STABILITY, BARKING, GB, vol. 95, no. 12, 1 December 2010 (2010-12-01), pages 2213 - 2225, XP027527376, ISSN: 0141-3910, [retrieved on 20100826] * |
HÜSNÜGÜL ATAY ET AL: "Turkish huntite/hydromagnesite mineral as a flame retardant in plastics", SOCIETY OF PLASTICS ENGINEERS PLASTICS RESEARCH ONLINE 10.1002/SPEPRO.002595, 1 January 2010 (2010-01-01), XP055026359, Retrieved from the Internet <URL:http://www.4spepro.org/pdf/002595/002595.pdf> [retrieved on 20120507], DOI: 10.1002/spepro.002595 * |
HÜSNÜGÜL YILMAZ ATAY ET AL: "Use of Turkish huntite/hydromagnesite mineral in plastic materials as a flame retardant", POLYMER COMPOSITES, vol. 31, no. 10, 16 February 2010 (2010-02-16), pages 1692 - 1700, XP055026451, ISSN: 0272-8397, DOI: 10.1002/pc.20959 * |
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TR201101673A2 (en) | 2012-09-21 |
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